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潜在的脑型疟疾治疗方法:肌肉注射蒿甲醚与维生素D联合用药。

Potential cerebral malaria therapy: intramuscular arteether and vitamin D co-administration.

作者信息

Dwivedi Hemlata, Singh Sunil Kumar, Chauhan Bhavana Singh, Gunjan Sarika, Tripathi Renu

机构信息

Division of Parasitology,CSIR-Central Drug Research Institute,Lucknow,Uttar Pradesh 226031,India.

出版信息

Parasitology. 2016 Oct;143(12):1557-68. doi: 10.1017/S0031182016001207. Epub 2016 Jul 21.

DOI:10.1017/S0031182016001207
PMID:27440106
Abstract

Cerebral malaria (CM) shows lethality rate of 15-25% despite effective antimalarial chemotherapy. The effective adjunct treatment to counteract the CM pathogenesis is urgently required. In murine CM model, most interventions studied till date are administered before the onset of CM symptoms, which belittle its translational value to human. We studied intramuscular arteether-vitamin D (ART-VD) combination treatment for CM outcome improvement after the onset of neurological symptoms. The intramuscular dose of 50 µg kg-1 VD for 3 days combined with a loading dose of 25 mg kg-1 α/β arteether followed by 12·5 mg kg-1 dose for two consecutive days led to significant improvement in survival (73% in combination group vs 29 and 0% in arteether and VD monotherapy, respectively) and clinical recovery. The treatment in all the groups partially restored the blood-brain barrier integrity and reduced the level of serum proinflammatory cytokines tumour necrosis factor-α and interferon-γ. The brain transcripts of inflammatory chemokines viz. CXCL10, CXCL9, CCL4 and CCL5 and T cell migration in the brain microvasculature were significantly diminished in all the treatment groups. ART-VD treatment significantly reduced intercellular cell adhesion molecule-1 expression. Taken together, our findings show that coordinated actions of ART-VD improve the outcome of experimental CM.

摘要

尽管有有效的抗疟化疗,但脑型疟疾(CM)的致死率仍为15%至25%。迫切需要有效的辅助治疗来对抗CM的发病机制。在小鼠CM模型中,迄今为止研究的大多数干预措施都是在CM症状出现之前进行的,这降低了其对人类的转化价值。我们研究了在神经症状出现后,肌肉注射蒿甲醚-维生素D(ART-VD)联合治疗对改善CM结局的作用。肌肉注射剂量为50 μg kg-1的VD,持续3天,联合25 mg kg-1的α/β蒿甲醚负荷剂量,随后连续两天给予12.5 mg kg-1的剂量,可显著提高生存率(联合治疗组为73%,而蒿甲醚单药治疗组和VD单药治疗组分别为29%和0%)并促进临床恢复。所有组的治疗都部分恢复了血脑屏障的完整性,并降低了血清促炎细胞因子肿瘤坏死因子-α和干扰素-γ的水平。所有治疗组中,炎症趋化因子即CXCL10、CXCL9、CCL4和CCL5的脑转录本以及脑微血管中的T细胞迁移均显著减少。ART-VD治疗显著降低了细胞间黏附分子-1的表达。综上所述,我们的研究结果表明,ART-VD的协同作用可改善实验性CM的结局。

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